Name: rs61486308
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs61486308

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr18:74110165-74110181 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: delTATA / delTA / dupTA / dupTATA …
delTATA / delTA / dupTA / dupTATA / dup(TA)₃ / dup(TA)₄ / dup(TA)₅
Variation Type: Indel Insertion and Deletion
Frequency: delTATA=0.0000 (0/5152, ALFA)
delTA=0.0000 (0/5152, ALFA)
dupTA=0.0000 (0/5152, ALFA) (+ 5 more)
dupTATA=0.0000 (0/5152, ALFA)
dup(TA)₃=0.0000 (0/5152, ALFA)
dup(TA)₄=0.0000 (0/5152, ALFA)
dup(TA)₅=0.0000 (0/5152, ALFA)
dupTA=0.17 (7/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: FBXO15 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	HWEP
Total	Global	5152	ATATATATATATATATA=1.0000	ATATATATATATA=0.0000, ATATATATATATATA=0.0000, ATATATATATATATATATA=0.0000, ATATATATATATATATATATA=0.0000, ATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATATA=0.0000	1.0	N/A
European	Sub	2650	ATATATATATATATATA=1.0000	ATATATATATATA=0.0000, ATATATATATATATA=0.0000, ATATATATATATATATATA=0.0000, ATATATATATATATATATATA=0.0000, ATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATATA=0.0000	1.0	N/A
African	Sub	1926	ATATATATATATATATA=1.0000	ATATATATATATA=0.0000, ATATATATATATATA=0.0000, ATATATATATATATATATA=0.0000, ATATATATATATATATATATA=0.0000, ATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATATA=0.0000	1.0	N/A
African Others	Sub	74	ATATATATATATATATA=1.00	ATATATATATATA=0.00, ATATATATATATATA=0.00, ATATATATATATATATATA=0.00, ATATATATATATATATATATA=0.00, ATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATA=0.00	1.0	N/A
African American	Sub	1852	ATATATATATATATATA=1.0000	ATATATATATATA=0.0000, ATATATATATATATA=0.0000, ATATATATATATATATATA=0.0000, ATATATATATATATATATATA=0.0000, ATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATATA=0.0000	1.0	N/A
Asian	Sub	76	ATATATATATATATATA=1.00	ATATATATATATA=0.00, ATATATATATATATA=0.00, ATATATATATATATATATA=0.00, ATATATATATATATATATATA=0.00, ATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATA=0.00	1.0	N/A
East Asian	Sub	56	ATATATATATATATATA=1.00	ATATATATATATA=0.00, ATATATATATATATA=0.00, ATATATATATATATATATA=0.00, ATATATATATATATATATATA=0.00, ATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATA=0.00	1.0	N/A
Other Asian	Sub	20	ATATATATATATATATA=1.00	ATATATATATATA=0.00, ATATATATATATATA=0.00, ATATATATATATATATATA=0.00, ATATATATATATATATATATA=0.00, ATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATA=0.00	1.0	N/A
Latin American 1	Sub	66	ATATATATATATATATA=1.00	ATATATATATATA=0.00, ATATATATATATATA=0.00, ATATATATATATATATATA=0.00, ATATATATATATATATATATA=0.00, ATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATA=0.00	1.0	N/A
Latin American 2	Sub	184	ATATATATATATATATA=1.000	ATATATATATATA=0.000, ATATATATATATATA=0.000, ATATATATATATATATATA=0.000, ATATATATATATATATATATA=0.000, ATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATA=0.000	1.0	N/A
South Asian	Sub	54	ATATATATATATATATA=1.00	ATATATATATATA=0.00, ATATATATATATATA=0.00, ATATATATATATATATATA=0.00, ATATATATATATATATATATA=0.00, ATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATA=0.00	1.0	N/A
Other	Sub	196	ATATATATATATATATA=1.000	ATATATATATATA=0.000, ATATATATATATATA=0.000, ATATATATATATATATATA=0.000, ATATATATATATATATATATA=0.000, ATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATA=0.000	1.0	N/A

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	5152	(AT)₈A=1.0000	delTATA=0.0000, delTA=0.0000, dupTA=0.0000, dupTATA=0.0000, dup(TA)₃=0.0000, dup(TA)₄=0.0000, dup(TA)₅=0.0000
Allele Frequency Aggregator	European	Sub	2650	(AT)₈A=1.0000	delTATA=0.0000, delTA=0.0000, dupTA=0.0000, dupTATA=0.0000, dup(TA)₃=0.0000, dup(TA)₄=0.0000, dup(TA)₅=0.0000
Allele Frequency Aggregator	African	Sub	1926	(AT)₈A=1.0000	delTATA=0.0000, delTA=0.0000, dupTA=0.0000, dupTATA=0.0000, dup(TA)₃=0.0000, dup(TA)₄=0.0000, dup(TA)₅=0.0000
Allele Frequency Aggregator	Other	Sub	196	(AT)₈A=1.000	delTATA=0.000, delTA=0.000, dupTA=0.000, dupTATA=0.000, dup(TA)₃=0.000, dup(TA)₄=0.000, dup(TA)₅=0.000
Allele Frequency Aggregator	Latin American 2	Sub	184	(AT)₈A=1.000	delTATA=0.000, delTA=0.000, dupTA=0.000, dupTATA=0.000, dup(TA)₃=0.000, dup(TA)₄=0.000, dup(TA)₅=0.000
Allele Frequency Aggregator	Asian	Sub	76	(AT)₈A=1.00	delTATA=0.00, delTA=0.00, dupTA=0.00, dupTATA=0.00, dup(TA)₃=0.00, dup(TA)₄=0.00, dup(TA)₅=0.00
Allele Frequency Aggregator	Latin American 1	Sub	66	(AT)₈A=1.00	delTATA=0.00, delTA=0.00, dupTA=0.00, dupTATA=0.00, dup(TA)₃=0.00, dup(TA)₄=0.00, dup(TA)₅=0.00
Allele Frequency Aggregator	South Asian	Sub	54	(AT)₈A=1.00	delTATA=0.00, delTA=0.00, dupTA=0.00, dupTATA=0.00, dup(TA)₃=0.00, dup(TA)₄=0.00, dup(TA)₅=0.00
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupTA=0.17

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 18	NC_000018.10:g.74110166TA[6]
GRCh38.p14 chr 18	NC_000018.10:g.74110166TA[7]
GRCh38.p14 chr 18	NC_000018.10:g.74110166TA[9]
GRCh38.p14 chr 18	NC_000018.10:g.74110166TA[10]
GRCh38.p14 chr 18	NC_000018.10:g.74110166TA[11]
GRCh38.p14 chr 18	NC_000018.10:g.74110166TA[12]
GRCh38.p14 chr 18	NC_000018.10:g.74110166TA[13]
GRCh37.p13 chr 18	NC_000018.9:g.71777401TA[6]
GRCh37.p13 chr 18	NC_000018.9:g.71777401TA[7]
GRCh37.p13 chr 18	NC_000018.9:g.71777401TA[9]
GRCh37.p13 chr 18	NC_000018.9:g.71777401TA[10]
GRCh37.p13 chr 18	NC_000018.9:g.71777401TA[11]
GRCh37.p13 chr 18	NC_000018.9:g.71777401TA[12]
GRCh37.p13 chr 18	NC_000018.9:g.71777401TA[13]

Gene: FBXO15, F-box protein 15 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
FBXO15 transcript variant 2	NM_001142958.2:c.1138+131… NM_001142958.2:c.1138+13188AT[6]	N/A	Intron Variant
FBXO15 transcript variant 1	NM_152676.3:c.910+13188AT… NM_152676.3:c.910+13188AT[6]	N/A	Intron Variant
FBXO15 transcript variant X1	XM_011525856.2:c.928+1318… XM_011525856.2:c.928+13188AT[6]	N/A	Intron Variant
FBXO15 transcript variant X8	XM_011525860.1:c.785+1922… XM_011525860.1:c.785+19225AT[6]	N/A	Intron Variant
FBXO15 transcript variant X3	XM_017025604.3:c.910+1318… XM_017025604.3:c.910+13188AT[6]	N/A	Intron Variant
FBXO15 transcript variant X4	XM_047437341.1:c.910+1318… XM_047437341.1:c.910+13188AT[6]	N/A	Intron Variant
FBXO15 transcript variant X5	XM_047437342.1:c.910+1318… XM_047437342.1:c.910+13188AT[6]	N/A	Intron Variant
FBXO15 transcript variant X6	XM_011525858.2:c.	N/A	Genic Downstream Transcript Variant
FBXO15 transcript variant X2	XM_024451099.2:c.	N/A	Genic Downstream Transcript Variant
FBXO15 transcript variant X7	XM_047437343.1:c.	N/A	Genic Downstream Transcript Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(AT)₈A=	delTATA	delTA	dupTA	dupTATA	dup(TA)₃	dup(TA)₄	dup(TA)₅
GRCh38.p14 chr 18	NC_000018.10:g.74110165_74110181=	NC_000018.10:g.74110166TA[6]	NC_000018.10:g.74110166TA[7]	NC_000018.10:g.74110166TA[9]	NC_000018.10:g.74110166TA[10]	NC_000018.10:g.74110166TA[11]	NC_000018.10:g.74110166TA[12]	NC_000018.10:g.74110166TA[13]
GRCh37.p13 chr 18	NC_000018.9:g.71777400_71777416=	NC_000018.9:g.71777401TA[6]	NC_000018.9:g.71777401TA[7]	NC_000018.9:g.71777401TA[9]	NC_000018.9:g.71777401TA[10]	NC_000018.9:g.71777401TA[11]	NC_000018.9:g.71777401TA[12]	NC_000018.9:g.71777401TA[13]
FBXO15 transcript variant 2	NM_001142958.1:c.1138+13203=	NM_001142958.1:c.1138+13188AT[6]	NM_001142958.1:c.1138+13188AT[7]	NM_001142958.1:c.1138+13188AT[9]	NM_001142958.1:c.1138+13188AT[10]	NM_001142958.1:c.1138+13188AT[11]	NM_001142958.1:c.1138+13188AT[12]	NM_001142958.1:c.1138+13188AT[13]
FBXO15 transcript variant 2	NM_001142958.2:c.1138+13203=	NM_001142958.2:c.1138+13188AT[6]	NM_001142958.2:c.1138+13188AT[7]	NM_001142958.2:c.1138+13188AT[9]	NM_001142958.2:c.1138+13188AT[10]	NM_001142958.2:c.1138+13188AT[11]	NM_001142958.2:c.1138+13188AT[12]	NM_001142958.2:c.1138+13188AT[13]
FBXO15 transcript variant 1	NM_152676.2:c.910+13203=	NM_152676.2:c.910+13188AT[6]	NM_152676.2:c.910+13188AT[7]	NM_152676.2:c.910+13188AT[9]	NM_152676.2:c.910+13188AT[10]	NM_152676.2:c.910+13188AT[11]	NM_152676.2:c.910+13188AT[12]	NM_152676.2:c.910+13188AT[13]
FBXO15 transcript variant 1	NM_152676.3:c.910+13203=	NM_152676.3:c.910+13188AT[6]	NM_152676.3:c.910+13188AT[7]	NM_152676.3:c.910+13188AT[9]	NM_152676.3:c.910+13188AT[10]	NM_152676.3:c.910+13188AT[11]	NM_152676.3:c.910+13188AT[12]	NM_152676.3:c.910+13188AT[13]
FBXO15 transcript variant X1	XM_011525856.2:c.928+13203=	XM_011525856.2:c.928+13188AT[6]	XM_011525856.2:c.928+13188AT[7]	XM_011525856.2:c.928+13188AT[9]	XM_011525856.2:c.928+13188AT[10]	XM_011525856.2:c.928+13188AT[11]	XM_011525856.2:c.928+13188AT[12]	XM_011525856.2:c.928+13188AT[13]
FBXO15 transcript variant X8	XM_011525860.1:c.785+19240=	XM_011525860.1:c.785+19225AT[6]	XM_011525860.1:c.785+19225AT[7]	XM_011525860.1:c.785+19225AT[9]	XM_011525860.1:c.785+19225AT[10]	XM_011525860.1:c.785+19225AT[11]	XM_011525860.1:c.785+19225AT[12]	XM_011525860.1:c.785+19225AT[13]
FBXO15 transcript variant X3	XM_017025604.3:c.910+13203=	XM_017025604.3:c.910+13188AT[6]	XM_017025604.3:c.910+13188AT[7]	XM_017025604.3:c.910+13188AT[9]	XM_017025604.3:c.910+13188AT[10]	XM_017025604.3:c.910+13188AT[11]	XM_017025604.3:c.910+13188AT[12]	XM_017025604.3:c.910+13188AT[13]
FBXO15 transcript variant X4	XM_047437341.1:c.910+13203=	XM_047437341.1:c.910+13188AT[6]	XM_047437341.1:c.910+13188AT[7]	XM_047437341.1:c.910+13188AT[9]	XM_047437341.1:c.910+13188AT[10]	XM_047437341.1:c.910+13188AT[11]	XM_047437341.1:c.910+13188AT[12]	XM_047437341.1:c.910+13188AT[13]
FBXO15 transcript variant X5	XM_047437342.1:c.910+13203=	XM_047437342.1:c.910+13188AT[6]	XM_047437342.1:c.910+13188AT[7]	XM_047437342.1:c.910+13188AT[9]	XM_047437342.1:c.910+13188AT[10]	XM_047437342.1:c.910+13188AT[11]	XM_047437342.1:c.910+13188AT[12]	XM_047437342.1:c.910+13188AT[13]

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

53 SubSNP, 25 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss81503258	Dec 03, 2013 (138)
2	HGSV	ss81563765	Dec 04, 2013 (138)
3	GMI	ss289367918	May 04, 2012 (137)
4	SSMP	ss664418327	Apr 01, 2015 (144)
5	SSIP	ss947385930	Aug 21, 2014 (142)
6	DDI	ss1536878814	Jan 10, 2018 (151)
7	EVA_GENOME_DK	ss1575195607	Apr 01, 2015 (144)
8	EVA_UK10K_ALSPAC	ss1709065284	Apr 01, 2015 (144)
9	EVA_UK10K_ALSPAC	ss1709065285	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1709067410	Apr 01, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1709067411	Apr 01, 2015 (144)
12	PADH-LAB_SPU	ss1713971796	Sep 08, 2015 (146)
13	SWEGEN	ss3016843225	Nov 08, 2017 (151)
14	SWEGEN	ss3016843226	Nov 08, 2017 (151)
15	SWEGEN	ss3016843227	Nov 08, 2017 (151)
16	MCHAISSO	ss3064747175	Nov 08, 2017 (151)
17	EVA_DECODE	ss3702045506	Jul 13, 2019 (153)
18	EVA_DECODE	ss3702045507	Jul 13, 2019 (153)
19	EVA_DECODE	ss3702045508	Jul 13, 2019 (153)
20	EVA_DECODE	ss3702045509	Jul 13, 2019 (153)
21	EVA_DECODE	ss3702045510	Jul 13, 2019 (153)
22	ACPOP	ss3742722745	Jul 13, 2019 (153)
23	ACPOP	ss3742722746	Jul 13, 2019 (153)
24	PACBIO	ss3788428029	Jul 13, 2019 (153)
25	PACBIO	ss3793352113	Jul 13, 2019 (153)
26	PACBIO	ss3798238590	Jul 13, 2019 (153)
27	EVA	ss3835273665	Apr 27, 2020 (154)
28	GNOMAD	ss4325322473	Apr 26, 2021 (155)
29	GNOMAD	ss4325322474	Apr 26, 2021 (155)
30	GNOMAD	ss4325322475	Apr 26, 2021 (155)
31	GNOMAD	ss4325322476	Apr 26, 2021 (155)
32	GNOMAD	ss4325322477	Apr 26, 2021 (155)
33	GNOMAD	ss4325322479	Apr 26, 2021 (155)
34	GNOMAD	ss4325322480	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5226031008	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5226031009	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5226031010	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5226031011	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5226031012	Apr 26, 2021 (155)
40	1000G_HIGH_COVERAGE	ss5305968643	Oct 16, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5305968644	Oct 16, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5305968645	Oct 16, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5305968646	Oct 16, 2022 (156)
44	HUGCELL_USP	ss5498676131	Oct 16, 2022 (156)
45	HUGCELL_USP	ss5498676132	Oct 16, 2022 (156)
46	HUGCELL_USP	ss5498676133	Oct 16, 2022 (156)
47	HUGCELL_USP	ss5498676134	Oct 16, 2022 (156)
48	HUGCELL_USP	ss5498676135	Oct 16, 2022 (156)
49	TOMMO_GENOMICS	ss5784065025	Oct 16, 2022 (156)
50	TOMMO_GENOMICS	ss5784065026	Oct 16, 2022 (156)
51	TOMMO_GENOMICS	ss5784065027	Oct 16, 2022 (156)
52	TOMMO_GENOMICS	ss5784065028	Oct 16, 2022 (156)
53	TOMMO_GENOMICS	ss5784065029	Oct 16, 2022 (156)
54	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 41659624 (NC_000018.9:71777399::AT 1112/3854) Row 41659625 (NC_000018.9:71777399::ATAT 298/3854)	-	Oct 12, 2018 (152)
55	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 41659624 (NC_000018.9:71777399::AT 1112/3854) Row 41659625 (NC_000018.9:71777399::ATAT 298/3854)	-	Oct 12, 2018 (152)
56	The Danish reference pan genome	NC_000018.9 - 71777400	Apr 27, 2020 (154)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 530062968 (NC_000018.10:74110164::AT 29605/118410) Row 530062969 (NC_000018.10:74110164::ATAT 12591/118464) Row 530062970 (NC_000018.10:74110164::ATATAT 245/118612)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 530062968 (NC_000018.10:74110164::AT 29605/118410) Row 530062969 (NC_000018.10:74110164::ATAT 12591/118464) Row 530062970 (NC_000018.10:74110164::ATATAT 245/118612)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 530062968 (NC_000018.10:74110164::AT 29605/118410) Row 530062969 (NC_000018.10:74110164::ATAT 12591/118464) Row 530062970 (NC_000018.10:74110164::ATATAT 245/118612)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 530062968 (NC_000018.10:74110164::AT 29605/118410) Row 530062969 (NC_000018.10:74110164::ATAT 12591/118464) Row 530062970 (NC_000018.10:74110164::ATATAT 245/118612)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 530062968 (NC_000018.10:74110164::AT 29605/118410) Row 530062969 (NC_000018.10:74110164::ATAT 12591/118464) Row 530062970 (NC_000018.10:74110164::ATATAT 245/118612)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 530062968 (NC_000018.10:74110164::AT 29605/118410) Row 530062969 (NC_000018.10:74110164::ATAT 12591/118464) Row 530062970 (NC_000018.10:74110164::ATATAT 245/118612)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 530062968 (NC_000018.10:74110164::AT 29605/118410) Row 530062969 (NC_000018.10:74110164::ATAT 12591/118464) Row 530062970 (NC_000018.10:74110164::ATATAT 245/118612)...	-	Apr 26, 2021 (155)
64	Northern Sweden Submission ignored due to conflicting rows: Row 16007610 (NC_000018.9:71777399::AT 225/600) Row 16007611 (NC_000018.9:71777399::ATAT 79/600)	-	Jul 13, 2019 (153)
65	Northern Sweden Submission ignored due to conflicting rows: Row 16007610 (NC_000018.9:71777399::AT 225/600) Row 16007611 (NC_000018.9:71777399::ATAT 79/600)	-	Jul 13, 2019 (153)
66	8.3KJPN Submission ignored due to conflicting rows: Row 84000315 (NC_000018.9:71777399::ATAT 3070/16760) Row 84000316 (NC_000018.9:71777399::AT 2722/16760) Row 84000317 (NC_000018.9:71777399:AT: 19/16760)...	-	Apr 26, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 84000315 (NC_000018.9:71777399::ATAT 3070/16760) Row 84000316 (NC_000018.9:71777399::AT 2722/16760) Row 84000317 (NC_000018.9:71777399:AT: 19/16760)...	-	Apr 26, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 84000315 (NC_000018.9:71777399::ATAT 3070/16760) Row 84000316 (NC_000018.9:71777399::AT 2722/16760) Row 84000317 (NC_000018.9:71777399:AT: 19/16760)...	-	Apr 26, 2021 (155)
69	8.3KJPN Submission ignored due to conflicting rows: Row 84000315 (NC_000018.9:71777399::ATAT 3070/16760) Row 84000316 (NC_000018.9:71777399::AT 2722/16760) Row 84000317 (NC_000018.9:71777399:AT: 19/16760)...	-	Apr 26, 2021 (155)
70	8.3KJPN Submission ignored due to conflicting rows: Row 84000315 (NC_000018.9:71777399::ATAT 3070/16760) Row 84000316 (NC_000018.9:71777399::AT 2722/16760) Row 84000317 (NC_000018.9:71777399:AT: 19/16760)...	-	Apr 26, 2021 (155)
71	14KJPN Submission ignored due to conflicting rows: Row 117902129 (NC_000018.10:74110164::AT 4600/28258) Row 117902130 (NC_000018.10:74110164::ATAT 5130/28258) Row 117902131 (NC_000018.10:74110164:AT: 33/28258)...	-	Oct 16, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 117902129 (NC_000018.10:74110164::AT 4600/28258) Row 117902130 (NC_000018.10:74110164::ATAT 5130/28258) Row 117902131 (NC_000018.10:74110164:AT: 33/28258)...	-	Oct 16, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 117902129 (NC_000018.10:74110164::AT 4600/28258) Row 117902130 (NC_000018.10:74110164::ATAT 5130/28258) Row 117902131 (NC_000018.10:74110164:AT: 33/28258)...	-	Oct 16, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 117902129 (NC_000018.10:74110164::AT 4600/28258) Row 117902130 (NC_000018.10:74110164::ATAT 5130/28258) Row 117902131 (NC_000018.10:74110164:AT: 33/28258)...	-	Oct 16, 2022 (156)
75	14KJPN Submission ignored due to conflicting rows: Row 117902129 (NC_000018.10:74110164::AT 4600/28258) Row 117902130 (NC_000018.10:74110164::ATAT 5130/28258) Row 117902131 (NC_000018.10:74110164:AT: 33/28258)...	-	Oct 16, 2022 (156)
76	UK 10K study - Twins Submission ignored due to conflicting rows: Row 41659624 (NC_000018.9:71777399::AT 1070/3708) Row 41659625 (NC_000018.9:71777399::ATAT 268/3708)	-	Oct 12, 2018 (152)
77	UK 10K study - Twins Submission ignored due to conflicting rows: Row 41659624 (NC_000018.9:71777399::AT 1070/3708) Row 41659625 (NC_000018.9:71777399::ATAT 268/3708)	-	Oct 12, 2018 (152)
78	ALFA	NC_000018.10 - 74110165	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs150086540	May 04, 2012 (137)
rs370293129	May 13, 2013 (138)
rs375128677	May 15, 2013 (138)
rs796962485	Nov 08, 2017 (151)
rs796769676	Nov 08, 2017 (151)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4325322480	NC_000018.10:74110164:ATAT:	NC_000018.10:74110164:ATATATATATAT… NC_000018.10:74110164:ATATATATATATATATA:ATATATATATATA	(self)
971612257	NC_000018.10:74110164:ATATATATATAT… NC_000018.10:74110164:ATATATATATATATATA:ATATATATATATA	NC_000018.10:74110164:ATATATATATAT… NC_000018.10:74110164:ATATATATATATATATA:ATATATATATATA	(self)
ss3702045506	NC_000018.10:74110177:TATA:	NC_000018.10:74110164:ATATATATATAT… NC_000018.10:74110164:ATATATATATATATATA:ATATATATATATA	(self)
ss1536878814, ss5226031010	NC_000018.9:71777399:AT:	NC_000018.10:74110164:ATATATATATAT… NC_000018.10:74110164:ATATATATATATATATA:ATATATATATATATA	(self)
ss4325322479, ss5305968645, ss5498676131, ss5784065027	NC_000018.10:74110164:AT:	NC_000018.10:74110164:ATATATATATAT… NC_000018.10:74110164:ATATATATATATATATA:ATATATATATATATA	(self)
971612257	NC_000018.10:74110164:ATATATATATAT… NC_000018.10:74110164:ATATATATATATATATA:ATATATATATATATA	NC_000018.10:74110164:ATATATATATAT… NC_000018.10:74110164:ATATATATATATATATA:ATATATATATATATA	(self)
ss3702045507	NC_000018.10:74110179:TA:	NC_000018.10:74110164:ATATATATATAT… NC_000018.10:74110164:ATATATATATATATATA:ATATATATATATATA	(self)
610974, ss664418327, ss1575195607, ss1709065284, ss1709067410, ss1713971796, ss3016843226, ss3742722745, ss3788428029, ss3793352113, ss3798238590, ss3835273665, ss5226031009	NC_000018.9:71777399::AT	NC_000018.10:74110164:ATATATATATAT… NC_000018.10:74110164:ATATATATATATATATA:ATATATATATATATATATA	(self)
ss4325322473, ss5305968644, ss5498676132, ss5784065025	NC_000018.10:74110164::AT	NC_000018.10:74110164:ATATATATATAT… NC_000018.10:74110164:ATATATATATATATATA:ATATATATATATATATATA	(self)
971612257	NC_000018.10:74110164:ATATATATATAT… NC_000018.10:74110164:ATATATATATATATATA:ATATATATATATATATATA	NC_000018.10:74110164:ATATATATATAT… NC_000018.10:74110164:ATATATATATATATATA:ATATATATATATATATATA	(self)
ss3702045508	NC_000018.10:74110181::TA	NC_000018.10:74110164:ATATATATATAT… NC_000018.10:74110164:ATATATATATATATATA:ATATATATATATATATATA	(self)
ss81503258, ss81563765	NT_025028.14:19568280::TA	NC_000018.10:74110164:ATATATATATAT… NC_000018.10:74110164:ATATATATATATATATA:ATATATATATATATATATA	(self)
ss289367918	NC_000018.8:69928396::TATA	NC_000018.10:74110164:ATATATATATAT… NC_000018.10:74110164:ATATATATATATATATA:ATATATATATATATATATATA	(self)
ss947385930, ss1709065285, ss1709067411, ss3016843225, ss3742722746, ss5226031008	NC_000018.9:71777399::ATAT	NC_000018.10:74110164:ATATATATATAT… NC_000018.10:74110164:ATATATATATATATATA:ATATATATATATATATATATA	(self)
ss3064747175, ss4325322474, ss5305968643, ss5498676133, ss5784065026	NC_000018.10:74110164::ATAT	NC_000018.10:74110164:ATATATATATAT… NC_000018.10:74110164:ATATATATATATATATA:ATATATATATATATATATATA	(self)
971612257	NC_000018.10:74110164:ATATATATATAT… NC_000018.10:74110164:ATATATATATATATATA:ATATATATATATATATATATA	NC_000018.10:74110164:ATATATATATAT… NC_000018.10:74110164:ATATATATATATATATA:ATATATATATATATATATATA	(self)
ss3702045509	NC_000018.10:74110181::TATA	NC_000018.10:74110164:ATATATATATAT… NC_000018.10:74110164:ATATATATATATATATA:ATATATATATATATATATATA	(self)
ss3016843227, ss5226031011	NC_000018.9:71777399::ATATAT	NC_000018.10:74110164:ATATATATATAT… NC_000018.10:74110164:ATATATATATATATATA:ATATATATATATATATATATATA	(self)
ss4325322475, ss5305968646, ss5498676134, ss5784065028	NC_000018.10:74110164::ATATAT	NC_000018.10:74110164:ATATATATATAT… NC_000018.10:74110164:ATATATATATATATATA:ATATATATATATATATATATATA	(self)
971612257	NC_000018.10:74110164:ATATATATATAT… NC_000018.10:74110164:ATATATATATATATATA:ATATATATATATATATATATATA	NC_000018.10:74110164:ATATATATATAT… NC_000018.10:74110164:ATATATATATATATATA:ATATATATATATATATATATATA	(self)
ss3702045510	NC_000018.10:74110181::TATATA	NC_000018.10:74110164:ATATATATATAT… NC_000018.10:74110164:ATATATATATATATATA:ATATATATATATATATATATATA	(self)
ss5226031012	NC_000018.9:71777399::ATATATAT	NC_000018.10:74110164:ATATATATATAT… NC_000018.10:74110164:ATATATATATATATATA:ATATATATATATATATATATATATA	(self)
ss4325322476, ss5784065029	NC_000018.10:74110164::ATATATAT	NC_000018.10:74110164:ATATATATATAT… NC_000018.10:74110164:ATATATATATATATATA:ATATATATATATATATATATATATA	(self)
971612257	NC_000018.10:74110164:ATATATATATAT… NC_000018.10:74110164:ATATATATATATATATA:ATATATATATATATATATATATATA	NC_000018.10:74110164:ATATATATATAT… NC_000018.10:74110164:ATATATATATATATATA:ATATATATATATATATATATATATA	(self)
ss4325322477, ss5498676135	NC_000018.10:74110164::ATATATATAT	NC_000018.10:74110164:ATATATATATAT… NC_000018.10:74110164:ATATATATATATATATA:ATATATATATATATATATATATATATA	(self)
971612257	NC_000018.10:74110164:ATATATATATAT… NC_000018.10:74110164:ATATATATATATATATA:ATATATATATATATATATATATATATA	NC_000018.10:74110164:ATATATATATAT… NC_000018.10:74110164:ATATATATATATATATA:ATATATATATATATATATATATATATA	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs61486308

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs61486308